| UMLS CUI | C0012715 |
| UMLS Term | Iron Metabolism Disorders |
| MeSH ID | D019189 |
| MeSH Term | Iron Metabolism Disorders |
| Disease Classes |
Nutritional and Metabolic Diseases |
| Gene Symbol | Description | Entrez ID | Uniprot ID | Chromosomal Location |
|---|---|---|---|---|
|
FTL |
ferritin, light polypeptide |
2512 |
P02792 |
chr19: 48,965,301-48,966,878 |
|
HMOX1 |
heme oxygenase 1 |
3162 |
P09601 |
chr22: 35,380,361-35,394,214 |
|
TFRC |
transferrin receptor |
7037 |
P02786 |
chr3: 196,027,183-196,082,189 |